VACCINE COMBINATIONS

Abstract

Vaccine combinations which comprise at least two or more of the following antigens: DTap-HEV-HepB-HPV suitable for administration in humans. A number of variations in the combination of these antigens have been disclosed that is suitable for concomitant administration. The methods of preparing the vaccine combinations are disclosed. Nucleic acids encoding the antigens, as well as methods for their production and use are provided.

Description

FIELD OF INVENTION

[0001] The invention relates to a combination vaccine and uses thereof.

BACKGROUND OF THE INVENTION

[0002] The incidence of Human papillomavirus (HPV) infections is high in the developing countries. In India, more than 134,000 new cases and nearly 74,000 deaths due to cervical cancer are reported every year according to the report of the WHO/ICO HPV Information Centre, June 2010.

[0003] In India, cervical and breast cancer are most frequent among the cancer cases in women particularly in the age group of 15-44 years. About 7.9% of women in the general population harbor HPV infection and most incidences of invasive cervical cancers are caused by HPV16 and HPV18. Mixed infections with other HPV genotypes are common Candidate vaccines that confer broad protective efficacy against multiple genotypes is the way forward for effective HPV vaccination. The HPV vaccines using the L1 capsid proteins are type specific for HPV16, HPV18, HPV6 and HPV11 and fail to offer complete protection against infection caused by other genotypes such as HPV31, HPV35, HPV52, HPV58 etc. which are also associated with progression of HPV infection to cervical carcinoma. There are no HPV vaccines available commercially as yet, that offers cross protection against infection by multiple HPV genotypes. Two preventive vaccines comprising recombinant HPV L1 virus-like particles (VLPs) have been licensed. They target only two of the approximately 15 known oncogenic HPV types. Nearly 70% of cervical cancer cases are attributed to HPV16 and HPV18, and there is evidence for some degree of cross-protection against the other closely related genotypes of HPV. Other approaches to the development of broadly protective HPV vaccines include multivalent vaccines using L1 capsid protein of at least nine HPV oncogenic viruses, with no added cost advantage and hence the cost of these vaccines would preclude sustained global delivery particularly in third world countries where the incidence of HPV infection is high. Other approaches have used the HPV L1 antigens in combination with HPV L2 capsid protein which have broadly neutralizing epitopes. However, the L2 capsid protein is by itself poorly immunogenic necessitating alternate strategies of combining the epitopes derived from L2 protein in combination with HPV L1 capsid protein, or in combination with other viral antigens that have the ability to assemble into Virus-Like Particles (VLPs). The rationale for design of such chimeras is for increasing the epitope density of the heterologous peptides on the backbone of the VLPs thereby increasing their immunogenicity. Chimeric constructs of HPV16 L2 epitopes with the HbsAg (Hepatitis B surface antigen) to assemble into virus like particles (VLPs) has been described in PCT/IN2009/000333.

[0004] Hepatitis E virus (HEV) is an enterically transmitted virus that is responsible for endemic hepatitis as well as sporadic acute hepatitis. HEV-infected persons exhibit a wide clinical spectrum ranging from asymptomatic infection to fulminant hepatitis. The clinical features of hepatitis E virus with icterus, high fever, hepatomegaly, and pruritus are similar to those of acute viral hepatitis caused by other hepatotropic viruses. The viral infection is commonly diagnosed by laboratory findings of elevated serum bilirubin, increase in liver enzymes and mild increases in alkaline phosphatase activity. The incidence of HEV is high in the developing countries (Emerson and Purcell, 2007; Chandra et al., 2008). HEV is an important aetiological agent for sporadic fulminant hepatic failure (FHF) in developing countries [Nanda et al., 1994]. The HEV infection accounts for more than 50% of acute viral hepatitis cases with a case fatality of 0.2% to 4% in the general population and upto 20% in pregnant women especially during the third trimester of pregnancy (Guu et al., 2009). High mortality, particularly during the third trimester of pregnancy, following fulminant hepatic failure, is characteristic of HEV infection in pregnant women (Khuroo et al., 1981) and may be related to hormonal changes in pregnancy (Lindemann et al., 2010). In studies involving pregnant women, it was shown that HEV accounted for nearly 37% of acute viral hepatitis infection and 81% of cases of fulminant hepatitis (Beniwal et al., 2003). An obstetric complication, such as premature rupture of membranes and intrauterine growth restriction is common during HEV infection is pregnancy [Kumar et al., 2004]. In HEV infection during third trimester of pregnancy, death is usually due to fulminant hepatitis or obstetric complications (Tsega et al., 1993). Vertical transmission of the virus with consequent morbidity and mortality of infants is also common with third trimester hepatitis E infections (Khuroo et al., 1995). The reasons for high mortality in pregnant women have not been understood clearly. HEV infection may also be associated with severe disease in persons with preexisting liver disease [Kumar Acharya et al., 2007]. Chronic infection with HEV is rare, but is more frequent in HIV-infected persons [Dalton et al., 2009]. Hepatitis outbreaks in developing countries have been caused primarily by HEV genotype 1. Epidemic outbreaks in Mexico and Western Africa were caused by genotype 2. Sporadic cases in Asia were caused by genotype 4. So far only genotypes 1 and 2 have occurred in humans, whereas genotypes 3 and 4 have also been isolated in animals. HEV has only one serotype (Mushahwar, 2008) which means that a candidate vaccine of one genotype can cross protect infection caused by other genotypes of the HEV. The use of Hepatitis E virus antigens including the ORF2, either the full length or truncated protein is known in the prior art (Amini-Bavil-Olyaee et al., 2009). The use of HEV viral antigens as vaccine for prophylaxis of HEV infection has been disclosed. A recombinant vaccine of HEV ORF2 that has been produced in E. coli has also been found to be safe for administration in humans (Zhu et al., 2010). A combination of the Hepatitis E and HPV vaccines for comprehensive healthcare of women is not disclosed in the prior art. Hence it was required to be demonstrate experimentally the feasibility of developing a combination vaccine where there is no antigenic interference when the hepatitis virus and HPV antigens are administered concomitantly either as an admixture that is mixed extemporaneously or as a chimeric antigen that carries both the vaccine epitopes in a single polypeptide expressed as a virus like particle (VLP). The development and use of such combinations is not known in the prior art.

[0005] The common problem that is encountered in the development of chimeric vaccines with the other viral antigens is the limitation of the scaffold antigen to accommodate heterologous protein sequences without affecting the native structural conformation that is required for immunogenicity of both the vaccines, especially if it were to be assembled as a virus like particle. Apart from the scaffold antigen, the sequence and the structural conformation of the heterologous protein for preparing the chimeric antigen is important. Also critically important is the location on the scaffold antigen where the heterologous sequence is to be added. Hence these factors cannot be pre-determined until the chimeric constructs are made and tested. To put it simply, what works for a pair of antigens would not be identical to another pair of antigens and hence this information cannot be extrapolated from the prior art describing similar design of chimeric antigens. The full length ORF2 protein of Hepatitis E consists of 660 amino acids. The neutralizing epitopes of the virus are not present largely at the N-terminus and C-terminus of the protein. Large amino acid deletions at the N- and the C-terminus do not diminish the ability of the protein to assemble into VLPs. Rational design of HPV-HEV chimeras involve the insertion of the heterologous HPV L2 broadly neutralizing epitopes in any region of the HEV ORF2 protein that does not affect the native structure of the protein and without compromising the immunogenicity of both the viral antigens. The insertion of the HPV L2 epitopes of desired sequences into any region of the HEV ORF2 protein that does not diminish the ability of the HEV antigen to assemble into VLPs, and at the same time display the heterologous HPV L2 epitopes on the surface of the chimeric VLP would be an ideal choice for vaccines against both HPV and HEV. A combination of HEV antigens with HEV-HPVL2chimeric antigen and/or with the HPV16 and HPV18 L1 capsid antigens as an admixture of the two antigens is also a very effective vaccine combination. Addition of HbsAg or chimeric HbsAg-HPVL2 whose method of production is described in PCT/IN2009/000333 to the HEV and/or HEV-L2 antigens is also not known in the prior art. ORF3 of HEV which is also an immunogenic structural protein is a good vaccine candidate that can be included as an antigen in such a vaccine combination. The addition of Tdap or DTap (diphtheria toxoid, tetanus toxoid and acellular pertussis antigens) or DTwP, wherein the acellular pertussis antigens are replaced by whole cell pertussis antigens to the aforementioned vaccine antigens is also novel and is not described in the prior art. The discovery and development of such vaccine combination is also very significant for the reasons mentioned below.

[0006] The mortality rate due to neonatal tetanus is high globally and especially so in the developing countries. It is easily preventable as antibodies against tetanus toxin are actively transported by the placenta from the immunized mother to her fetus. This provides passive protection against tetanus during the neonatal period and for a few months following birth. The mortality rate due to neonatal tetanus can be reduced with immunization of pregnant women or in women of childbearing age. It has been demonstrated that the use of two or more doses of tetanus toxoid during pregnancy could prevent neonatal tetanus (Schofield et al., 1961) Tetanus toxoid vaccination of pregnant women has been included in the WHO's Expanded Program on Immunization. Similarly, vaccination with Tdap (tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis) vaccines is also recommended for pregnant women. It is recommended that one dose of Tdap be administered during the third trimester or late in the second trimester (after 20 weeks gestation). If not administered during pregnancy, Tdap should be administered immediately postpartum. When Tdap is administered during pregnancy, at time of delivery the mother will be protected, making her less likely to transmit pertussis to her infant, and transplacental maternal antibodies will likely protect the infant against pertussis in early life. The preferred schedule in pregnant women is two doses of Td separated by 4 weeks, and a dose of Tdap 6 months after the second dose (post-partum). It is recommended that adolescents and/or women of active child bearing age should receive a dose of Tdap preferably before pregnancy. Whole cell pertussis vaccine can also be administered in lieu of acellular pertussis vaccine. Hence Tdap and/or tetanus toxoid vaccines are a good option to be included in the combination vaccine for women along with HPV and HEV antigens.

[0007] Such a combination vaccine for Hepatitis E with tetanus toxoid or with Tdap with and without HPV antigens is novel and is not commercially available or it is disclosed in any prior art. In the current invention, methods are disclosed on the development of a combination vaccine of HEV and HPV. The rationale for combining the aforementioned antigens either in a single formulation as an admixture, or administered concomitantly is to improve the overall health outcome in women, as cervical cancer ranks high as the most frequent cause of cancer among women in India, and also for the fact that hepatitis E infection causes high mortality in pregnant women particularly in the third trimester of pregnancy. The HPV-HEV vaccine combination can be expected to decrease the mortality and morbidity due to HPV and HEV infections and to improve the overall health in this segment of the population and as recommended, vaccination with Tdap to pregnant women reduces infant mortality due to tetanus and pertussis. Such combination vaccines are not only useful to provide protection against multiple pathogens, but are very desirable as they reduce the number of immunizations required. Combination vaccines also help to lower the manufacturing and distribution cost, making the vaccines cost-effective and affordable. Affordability of vaccines increases acceptance and coverage rates. The use of suitable adjuvants in the vaccine formulations also reduces the amount of antigen required and helps in the manufacture of low-cost vaccines thus conferring a distinct economic advantage. No antigenic interference has been observed with the co-administration of all the aforementioned antigens and hence combination of different antigens can be made. For the production of recombinant antigens, Pichia pastoris as recombinant expression host is advantageous at industrial scale as it is cost effective for large scale manufacture compared to other eukaryotic expression systems. Recombinant proteins derived from Pichia pastoris have been successfully commercialized and have been found safe for human use. Use of this expression system for the manufacture of both the HPV and HEV antigens is therefore safe and highly cost-effective for production of vaccines for HPV and HEV.

OBJECT OF THE INVENTION

[0008] Primary object of the invention is to provide vaccine combinations for prophylaxis and treatment of viral and bacterial infections.

[0009] Another object of the invention is to provide a combined vaccine for HPV, HEV and Hepatitis B infections.

[0010] Another object of the invention is to provide a combination vaccine of HPV-HEV-Hepatitis B antigens additionally comprising tetanus toxoid and/or the trivalent tetanus toxoid and/or reduced diphtheria toxoid and/or pertussis vaccines.

[0011] Another object of the invention is to provide sequences of the recombinant antigens of and HEV and the chimeric HPV-HEV antigens.

[0012] Another object of the invention is to provide the methods of development of such combination vaccines.

[0013] A further object of the invention is to provide a method of testing such combination vaccines in mammals.

[0014] Another object of the invention is to provide adjuvanted vaccine compositions of the aforementioned antigens.

[0015] A further object of the invention is to provide the HPV and HEV antibodies for diagnosis of the HPV and HEV viral infections.

SUMMARY OF THE INVENTION

[0016] Accordingly, there are provided vaccine combinations of DTap-HEV-HepB-HPV antigens in a number of variations in the combinations of these antigens with tetanus toxoid and/or the trivalent tetanus toxoid and/or reduced diphtheria toxoid and/or pertussis antigens.

[0017] The invention provides vaccine composition of a combination of antigens of human papillomavirus (HPV) and hepatitis E (HEV) for the prophylaxis, treatment and diagnosis of HPV and Hepatitis E virus infections in mammals, particularly humans. Further, the combination of hepatitis B antigen, tetanus toxoid and/or Tdap (tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis) vaccine to the aforementioned vaccine combination is also within the scope of the invention.

[0018] Adjuvanted vaccine compositions of the aforementioned virus antigens offer high protective efficacy. Such combination vaccine may be supplied in one container in a single combined formulation suitable for injection, or in different such containers (vials). Such vaccine compositions are administered by mixing the required amount of antigens extemporaneously in a single container before administering to a host as an injection. The combination of the aforementioned vaccines with other viral and bacterial antigens is also within the scope of the invention.

[0019] In one embodiment, the invention provides combination vaccine of purified HPV16 and HPV18 L1 antigens with purified HEV ORF2 antigen.

[0020] In another embodiment, the invention provides combination of HPV16, HPV18 L1 proteins and HPV16L2-HbsAg chimeric antigen in combination with HEV antigen.

[0021] In another embodiment, the invention provides chimeric HEV-HPVL2, and HPV16 and HPV18 L1 antigens which are useful for the prophylaxis of both the viral infections.

[0022] In an exemplary embodiment, vaccine composition of the invention comprises: a diphtheria toxoid, `D`; a tetanus toxoid, `T`; pertussis antigens; recombinant hepatitis B virus surface antigen, HBsAg; recombinant human papillomavirus L1 antigens of HPV16 and HPV18; recombinant hepatitis E (HEV) ORF2 antigen; recombinant HPV L2 epitope in chimeric fusion with HBsAg or Hepatitis E (HEV) protein. No antigenic interference is observed with the combination of aforementioned antigens.

[0023] The vaccines of the invention can be prepared extemporaneously at the time of use by mixing together two components: (a) a first component comprising HEV, HPV and chimeric HEV or HBsAg antigens; and (b) a second component comprising Tdap.

[0024] The two components are filled separately and thus in general, the invention provides a kit comprising: (a) a first component comprising HEV, HPV and chimeric HEV or HBsAg antigens; and (b) a second component comprising Tdap.

[0025] Alternatively Tdap can be formulated in aluminum hydroxide and used as a single component vaccine.

[0026] If packaged separately, the mixing step will typically take place at the time of use. Thus the invention provides a process for preparing a vaccine composition of the invention, comprising the steps of (a) providing a first component comprising HEV, HPV and chimeric HEV or HBsAg antigens and (b) providing a second component comprising Tdap antigens (c) mixing the first and second components to give the vaccine.

BRIEF DESCRIPTION OF DRAWINGS

[0027] FIG. 1: PCR amplification of (1A) approximately ˜1.494 Kb of HEV ORF2 gene (1B) ˜110 bp (that includes the gene sequence, restriction enzyme sequence and the 5' overhang) corresponding to the amino acid SATQLYKTCKQAGTCPPDIIPKVEG of HPV16 L2 and ˜60 bp (that includes the gene sequence, restriction sequence and the 5' overhang) corresponding to the amino acid sequence LVEETSFIDAGAP of the HPV L2 epitopes by PCR using gene specific primers described in Example 1. The size of the amplified gene fragment is shown against the 1 Kb ladder fore HEV ORF2 nad against 100 bp ladder for HPVL2 fragment.

[0028] FIG. 2: 2A represents Expression of HEV ORF2 of SEQ ID NO. 4 in Pichia pastoris at 24 hrs and 120 hrs after induction (I) with methanol showing the expression of 54 kDa protein; UI--uninduced cells; 2B represents Expression of HEV-HPVL2 of SEQ ID NO. 6 in Pichia pastoris at 48 hrs and 120 hrs after induction (I) with methanol showing the expression of the 56 kD protein; UI--uninduced cells; M--is the medium range molecular size marker (Genei, Bangalore).

[0029] FIG. 3: 3A represents Purified recombinant 54 kD HEV ORF2 protein of SEQ ID NO.4 indicated by thick arrow; and 3B represents the purified recombinant chimeric 56 kD HEV-HPV16 L2 protein is indicated by thick arrow. The size of the molecular size markers is shown.

[0030] FIG. 4: Represents Transmission electron microscopy (TEM) of the chimeric HEV-HPV16L2 protein stained with uranyl acetate shows the assembly of the protein spontaneously into virus like particles. The size of the bar is 200 nm as shown in the bottom of the picture.

DETAILED DESCRIPTION OF THE INVENTION

[0031] Detailed embodiments of the present invention are disclosed herein below. However, it is to be understood that the disclosed embodiments are merely exemplary of the invention, which can be embodied in various forms. The scope of the invention is not limited to the disclosed embodiments and terms and phrases used herein are not intended to be limiting but rather to provide an understandable description of the invention. The invention is defined by claims appended hereto.

[0032] The invention relates to vaccine composition that includes a combination of antigens of human papillomavirus (HPV) and hepatitis E virus (HEV) for the prophylaxis and diagnosis of HPV and Hepatitis E virus infections in mammals, particularly humans. Addition of Hepatitis B antigen to the above combination is included in the scope of the invention. Furthermore, the combination of tetanus toxoid and/or Tdap (tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis) vaccine to the aforementioned vaccine combination is also within the scope of the invention. Such vaccine compositions are administered by mixing the antigens extemporaneously in a single container before administering to a host as an injection, or can be concomitantly administered in humans in two or more separate formulations that can be injected parenterally at different sites for eliciting immune response. A combination vaccine of the aforementioned antigens is supplied in a single container such as a vaccine vial or in a pre-filled syringe ready for injection. The combination of the aforementioned vaccines with other viral and bacterial antigens is also within the scope of the invention.

[0033] The invention also provides a process for preparing a combination vaccine that comprises (i) a hepatitis E (HEV) virus like particle, (ii) a chimeric protein of hepatitis B virus surface antigen HbsAg with HPV L2 protein (`HbsAg-HPVL2`), and/or chimeric HEV-HPV L2 chimeric protein (iii) HPV16 L1 and HPV18 L1 antigens (iv) tetanus toxoid (`T`), (iii) acellular pertussis antigens (`aP`), (vi) diphtheria toxoid (`D`) and the process includes the steps of (a) combining the HEV component to the chimeric HEV-HPVL2 component to get a bivalent component (b) combining the HEV antigen to the chimeric HbsAg-HPVL2 to get a bivalent component (a) combining the HEV component to HPV16 L1 and HPV18 L1 components to get a trivalent HEV-HPV16L1-HPV18L1 component (a) combining a trivalent HEV-HPV16L1-HPV18L1 component with a monovalent chimeric HEV-L2 component, to get a tetravalent HEV-HPV16L1-HPV18L1-HEV-L2 component; (b) combining a trivalent HEV-HPV16L1-HPV18L1 component with chimeric HbsAg-HPVL2 to get a tetravalent HEV-HPV16L1-HPV18L1-HbsAg-L2 component and (c) mixing the D-T-aP-component with either of the bivalent/trivalent/tetravalent components for a combination vaccine/or concomitantly administering the D-T-aP vaccine along with the viral vaccines parenterally to a mammalian host.

[0034] The HPV capsid antigens of the combination vaccine are highly immunogenic when expressed as recombinant proteins in a eukaryotic expression system and are purified therefrom. The HPV antigens are derived from the major capsid protein L1 that is expressed as virus like particles (VLPs). HPV antigens include two or more antigens selected from a list of `oncogenic` HPV types including HPV16, HPV18, HPV31, HPV33, HPV35, HPV39, HPV45, HPV51, HPV52, HPV56, HPV58, HPV59, HPV68 etc and could include the HPV L2 capsid protein from any of the above mentioned HPV types Chimeric protein of HPV L2 capsid and HbsAg is a good vaccine candidate for use in combination vaccine with HEV and other HPV antigens. Additions of heterologous viral and bacterial epitopes that are fused to the aforementioned vaccine antigens also augment the immunogenicity of the HPV vaccine.

[0035] The hepatitis E vaccine antigens are those encompassing the full length or the truncated sequence of Open Reading Frame 2 (ORF2) of protein which is a structural protein of the Hepatitis E virus. Truncations of the HEV full length ORF2 protein were made to result in better expression with increased stability and without compromising the immunogenicity of the candidate antigen to assemble into VLPs. Truncated sequences of the HEV ORF2 such as 112-608 amino acid region and alternatively 368-606 amino acids were so designed to accommodate heterologous viral sequences without compromising the structural conformity required for eliciting strong immune response. From the full length sequences of HEV ORF2 protein such as in SEQ ID NO.1 and the full length protein of HPV16 L2 such as in SEQ ID NO. 2, different truncated gene fragments that encompass the major neutralizing epitopes of both the antigens were generated by PCR and several chimeric constructs were made by ligating the fragments together. The HEV gene sequences can be derived from any HEV genotype such as genotypes 1-4. The different sequences of the chimeric antigens are within the scope of the invention. Such constructs code for the chimeric proteins of different molecular sizes. No antigenic interference was observed with the combination of aforementioned antigens. It was found that the vaccines of the invention can be prepared extemporaneously at the time of use by mixing together two components: (a) a first component comprising HEV, HPV and chimeric HEV or HBsAg antigens; and (b) a second component comprising Tdap. The two components are filled separately, and thus in general the invention provides a kit comprising: (a) a first component comprising HEV, HPV and chimeric HEV or HBsAg antigens; and (b) a second component comprising Tdap. Alternatively Tdap can be formulated in aluminum hydroxide and used as a single component vaccine along with the viral antigens. If packaged separately, the mixing step will typically take place at the time of use. Thus the invention provides a process for preparing a vaccine composition of the invention, comprising the steps of (a) providing a first component comprising HEV, HPV and chimeric HEV or HBsAg antigens and (b) providing a second component comprising Tdap antigens (c) mixing the first and second components to give the vaccine.

[0036] With the aforementioned combination vaccine it was possible, to obtain antibody titers against HPV and HEV virus approaching or equivalent to, or in excess of 100% of the titer obtained when the antigen is administered in isolation to animals. The combination vaccine elicited robust antibody levels against both HPV and HEV virus infections and no antigenic interference was observed. All the methods described in the invention are applicable to any genotype or genotypic variants/serotypes/strains of HPV and Hepatitis E virus. Within the scope of the invention are the compositions and methods of preparing and using the HPV and HEV antigens of defined sequence expressed as recombinant proteins or recombinant virus like particles in any prokaryotic or eukaryotic expression system. The gene sequences are the native viral sequences or synthetic genes that are codon optimized for expression in the host cells. The eukaryotic expression system of choice includes mammalian cells; baculovirus mediated expression in insect cells, and yeast cells of any species, most preferably Pichia pastoris or Saccharomyces cerevisiae. Pichia pastoris was found to express the aforementioned antigens to a high level. Optimization of the sequence for eukaryotic expression includes the presence of Kozak's consensus sequence such as (gcc)gccRccATGG at the 5' end of the gene, where the ATG is the initiation codon, or the use of yeast consensus sequence (5'-[A/T]TTTAT[A/G]TTT[A/T]-3'). For expression in Pichia pastoris, the synthetic gene sequences were codon optimized to further increase the expression levels. The aforementioned proteins were expressed either as intracellular protein and purified therefrom. Alternatively they can be expressed as secretary proteins and purified. Any suitable expression vector is selected from the list that includes but is not limited to pPIC3.5, pPIC3.5K, pA018, pPIC9, pPIC9K, PHIL D2 etc. for expression in yeast cells. Any plasmid vector suitable for expression in Saccharomyces cerevisiae or any other species of yeast are used. The yeast cells include the following but are not limited to Pichia pastoris, Saccharomyces spp, Hanensula polymorpha, Schizosaccharomyces spp, kluveromyces spp. Either of the Pichia pastoris strains such as GS115, KM71 and protease deficient strains such as SMD1168 or SMD1163 is used for recombinant expression. The aforementioned genes are cloned either in single copy or in more than one copy. The antibodies against the HPV and HEV virus antigens are used for developing methods for estimation of antigen content by ELISA and also for use as a reference standard while estimating vaccine antibody titer. They find application in diagnosis also.

[0037] Purification of the virus was achieved by physical or chemical means and preferably by a combination of both. Physical methods utilize the physical properties of the virus like particles such as density, size, mass, sedimentation coefficient etc. and include any of the following techniques but are not limited to: ultracentrifugation, density gradient centrifugation, ultrafiltration etc. Purification through chemical means employs methods such as adsorption/desorption through chemical or physiochemical reactions such as ion exchange chromatography, affinity chromatography, hydrophobic interaction chromatography, gel filtration chromatography, hydroxyapatite matrix, salting with inorganic salts one such example being ammonium sulphate, and by the use of proprietary Himax technology, organic salts, organic solvents, aluminum phosphate, aluminum hydroxide and organic compounds such as polyethylene glycol. Purification of the recombinant antigens of the virus was achieved by either one or a combination of two or more of the above mentioned methods.

[0038] The antigenic compositions of the above mentioned HPV-HEV vaccine and HPV-HEV and tetanus toxoid and Tdap vaccines were formulated in pharmaceutically acceptable carrier that is suitable for immunization in human. Furthermore, for adjuvanted vaccine formulations, suitable adjuvants were selected from the following list, which includes but is not limited to: aluminum hydroxide, aluminum phosphate; calcium phosphate; inulin of any polymorphic form, preferably gamma inulin; adjuvants containing inulin in combination with other organic and inorganic compounds such as aluminum hydroxide, aluminum phosphate, aluminum sulphate phosphate and calcium phosphate; liposomes, chitosan and complex carbohydrates such as dextran, dextrins, starch, mannans and glucomannans, galactomannans, beta-glucans, heparin, cellulose, pectins and pectinates, lectins and any other carbohydrates either synthetic or derived from any source, any biodegradable and biocompatible polymers, such as poly lactide and poly(lactide co-glycolides; PLG) or PLGA; any emulsions including but not limited to oil in water emulsions, other squalene based adjuvants, oil in water emulsion containing cholecalciferol, cholecalciferol by itself as an adjuvant, any water in oil emulsion; liposomes prepared with cholecalciferol as one of the ingredients along with other lipid soluble compounds; liposomes of other compositions; RIBI adjuvant systems, saponins including but not limited to QS-21, QuilA, tomatine, ISCOMs, ISCOMATRIX etc, lipopeptides, glycopeptides, lipopolysaccharides, muramyl dipeptides and any peptide based adjuvants, oligonucleotides, any TLR ligands as adjuvants, any cytokine, vitamins and non-toxic bacterial toxins etc. In addition to the above, any other organic and inorganic substances that have good immunopotentiating activity can be used as adjuvants either singly or in combinations to enhance the immunogenicity of the HPV-HEV combination vaccines. The vaccine combinations with alum elicited strong immunological response when administered parenterally, in animals. The methods and vaccine compositions containing vaccine adjuvants are within the scope of the invention.

[0039] For potency testing of the vaccine, the vaccine formulations were tested in mice and guinea pigs. The resultant serum was assayed in vitro by estimation of antibody titer by ELISA. Toxin neutralization test was used for evaluation of potency of tetanus toxoid and diphtheria toxoid by procedures well described in literature. Seroconversion was observed in the animals immunized with the vaccine formulations described in the present invention. No antigenic interference either due to combination of different antigens or by adjuvant was observed. The buffer used in the formulations is phosphate buffer Phosphate-citrate buffer or any other pharmaceutically acceptable buffer of appropriate pH can be used. 2-phenoxyethanol was used vaccine preservative; thiomerosol or any other vaccine preservative can be used. Alternatively the vaccine combination can be formulated without any vaccine preservative. The vaccines optionally contain stabilizer(s) etc. The excipients were selected from a list that includes but is not limited to non-reducing sugars, sugar alcohols such sorbitol and mannitol, glycerol, amino acids, human serum albumin, and a choice of adjuvant from the aforementioned list of adjuvants. A stable formulation of the immunogen either in a liquid or in a lyophilized form and after reconstitution in a pharmaceutically acceptable buffer or water is suitable for administration parenterally in human host. More specifically, for antigens of the present invention, a diagnostic assay with high sensitivity and specificity for detecting infection are provided. The methods in the scope of the invention are applicable to any genotype/genotypic variants/serotype/strain of HPV and hepatitis E viruses.

EXAMPLES

[0040] The invention is further described in following examples.

Example-1

Cloning and Recombinant Expression of Hepatitis E (HEV) Viral and Chimeric HEV-HPVL2 Antigens

[0041] A synthetic gene of the Hepatitis E ORF2 gene of amino acid sequence of SEQ ID NO.1 was amplified by PCR with 5'primer and 3' primer containing EcoR1 and Not1 restriction sites respectively to obtain a ˜1494 bp PCR fragment of SEQ ID NO.3 that encodes the protein of SEQ ID NO. 4. (see FIG. 1). The primers used for PCR amplification of the HEV gene are 5'-CATTTGAATTCACCATGGCCGTTGCACCTGCTCATGATAC-3' and 5'-TATCGCGGCCGCTCATTAAGCCAATGCAGAATGAGGAGC-3'.

[0042] The conditions for PCR amplification were denaturation at 94° C. for 45 seconds, annealing at 60° C. for 40 seconds and extension at 72° C. for 2.5 minutes for 30 cycles followed by final extension at 72° C. for 10 minutes. The reaction mix consisted of 1×Taq DNA polymerase buffer, 0.25 mM dNTPS, 20 picomoles of each primer and 1 U of Taq DNA polymerase (Genei) and 1 U of Pfu DNA polymerase (New England Biolabs). The PCR fragment was digested with EcoR1 and Not1, gel purified and used for ligation to EcoR1 and Not1 digested yeast vector pPIC3.5K (Invitrogen, Carlsbad, USA). The 1494 bp PCR fragment was used for the chimeric fusion with gene sequence for HPV16 L2 epitopes consisting of 14-37 amino acids of the sequence SATQLYKTCKQAGTCPPDIIPKVEG and/or 108-120 amino acids of the sequence LVEETSFIDAGAP of the HPV16 L2 protein of SEQ ID NO 2 Chimeric fusion of the gene sequence for HPV16 L2 epitope 14-37 amino acids generated SEQ ID NO. 5 encoding SEQ ID NO.6 when ligated to the 5'end of HEV gene, and SEQ ID NO.7 encoding SEQ ID NO.8 when it was ligated to the 3' end of the of the HEV ORF2 PCR fragment. The ligation was achieved with a BamH1 site located at either end of the primers for HEV or HPV L2 sequence. The following primers were used for amplification of 14-37 amino acids of the HPV16 L2 sequence for fusion at the N-terminus of the HEV ORF2 fragment: 5'-ATGTCGAATTCACCATGGCTGCAACTCAGTTGTATAAAAC-3' and 5'-ATCGAGGATCCTTGAACCTTTGGGATAATGTC-3'. For amplification and fusion at the C-terminus of the HEV ORF2 fragment, the following primers were used for HPV16 L2 PCR of the above region: 5'-ATGTCGGATCCTCTGCAACTCAGTTGTATAAAAC-3' and 5'-ATCGAGCGGCCGCTCATTAACCTTCAACCTTTGGGATAATGTC-3'. PCR primers that were designed to amplify the 5' TTGGTTGAAGAAACCTCCTTTATTGACGCTGGTGCTCCA-3' region of HPV16 L2 gene corresponding to the protein sequence LVEETSFIDAGAP also contained a BamH1 site for ligation of the two gene fragments. Chimeric fusion of the gene fragment encoding LVEETSFIDAGAP to the C-terminus of HEV ORF2 resulted in SEQ ID NO. 9 encoding SEQ ID NO.10. The SEQ ID NO.11 is nucleotide sequence of HEV ORF2 with HPV L2 14-37 amino acid region at the N-terminus and HPV16 L2 108-120 amino acids at the C-terminus. The corresponding protein sequence is SEQ ID NO.12. Similarly, for generating chimeric constructs of HEV ORF2 with the aforementioned HPV L2 sequences, PCR primers for amplification of the 1494 bp fragment also included a BamH1 site either at the end of the 5' region or at the 3'end of the gene fragment to facilitate ligation to the HPV L2 epitopes. Alternatively construction of chimeric constructs of Hepatitis E with HPV L2 protein, a 714 bp fragment (from 368-606 amino acids) of ORF2 was amplified by PCR and ligated to HPV16 L2 epitopes (region 14-37 amino acids and/or 108-120 amino acids) either at the N-terminus or at the C-terminus of the HEV PCR fragment. For ligation at the N-terminal end, the HEV fragment was amplified with the primer 5'-ACGTCGGATCCATCGCCCTTACATTGTTTAATTTG-3' and 5'-TATCGCGGCCGCTCATTAAGCCAATGCAGAATGAGGAGC-3' and for ligation at the C-terminal end of the HEV fragment, the HEV gene was amplified with 5'-AGCTCGAATTCACCATGGCCCTTACATTGTTTAATTTG-3' and 5'-ACTCAGGATCCTTATCAAGCCAATGCAGAATGAGGAGC-3'. The conditions for PCR amplification were denaturation at 94° C. for 45 seconds, annealing at 56° C.-62° C. for 40 seconds for various primer combinations and extension at 72° C. for 2 minutes for 30 cycles followed by final extension at 72° C. for 10 minutes with reagents of the same concentration as mentioned above for 1494 bp HEV ORF2 amplification. For the generation of the chimeric genes of HPV L2 and HEV, the PCR amplified genes were ligated after BamH1 digestion, further digested with EcoR1 and Not1 and ligated into the EcoR1 and Not1 digested pPIC3.5K yeast vector and transformed in E. coli DH5α. The recombinant plasmid DNA was isolated from transformed E. coli selected on 50 μg/ml ampicillin. The recombinant plasmid containing the HEV-HPVL2 chimeric gene was linearized with BglII and transformed in Pichia pastoris GS115 cells as per the standard yeast transformation protocols (Invitrogen, Carlsbad, USA).

Example-2

Purification of the HEV and HEV-HPV L2 Chimeric Proteins

[0043] The Pichia pastoris GS115 clones expressing the recombinant proteins of HEV and the HEV-L2 chimeric proteins were grown for 96 hours at 280 C and induced with 1% methanol every 24 hours and harvested at the end of 120 hours (FIG. 2). The cells were washed once with 50 mM Tris-HCl buffer pH 8.0 containing 2 mM EDTA, 10 mM NaCl, and lysed in the same buffer containing 0.05% Triton X-100. The cell lysate was centrifuged at 4000 rpm for 20 minutes and the cell supernatant containing the proteins were purified on a Q-sepharose column equilibrated with the same buffer. The proteins were eluted with a salt gradient containing 50 mM to 750 mM NaCl in the same buffer and the fractions containing the protein were pooled and checked on SDS-PAGE gel for the presence of 54 kDa band for the HEV protein and 56 kDa band for the chimeric HEV-HPV16 L2 protein. The fractions containing HEV proteins were concentrated using TFF system and the concentrate was loaded on Captocore700 gel filtration column equilibrated with 50 mM phosphate buffer, pH 7.2 containing 154 mM NaCl. The viruses like particles were collected in the flow through. The purity of the protein was checked on SDS-PAGE gel and found to be more than 95% pure (FIG. 3). The purified proteins were further characterized.

Example-3

Transmission Electron Microscopy

[0044] The purified viruses like particles (VLPs) were visualized by Transmission Electron microscopy (TEM) after negative staining with 2% uranyl acetate and is depicted in FIG. 4.

Example-4

Vaccine Formulations for Potency Testing

[0045] For potency testing, the following vaccine combinations each consisting of the purified vaccine antigen of the below mentioned concentrations and adjuvant(s) were prepared for immunization in mice: a) 30 μg of HEV ORF2 54 kDa protein, 40 μg HPV16 L1 protein, 20 μg HPV18 L1 protein, and 30 μg HbsAg-HPV L2/HEV-HPV L2 chimeric antigen all adsorbed on 1.5 mg of aluminum hydroxide and Tdap (tetanus toxoid, reduced diphtheria toxin and acellular pertussis) comprising formaldehyde detoxified 2.5 Lf units of diphtheria toxin (DT), 5 Lf units of tetanus toxoid (TT) and 8 μg of detoxified Pertussis toxin (PT), 8 μg filamentous hemagglutinin (FHA) and 2.5 μg of pertactin (PRN) all adsorbed individually on aluminum hydroxide. Alternatively aluminum phosphate at 1.5 mg can be used for the adsorption of all the above antigens except tetanus toxoid that is adsorbed in aluminum hydroxide. The tetanus toxoid (TT) and detoxified Pertussis toxin (PT) are GMP products obtained from the production facility of Bharat Biotech Intl Ltd. The acellular pertussis antigens were purified from the culture supernatant of Bordetella pertussis though steps involving concentration of the culture supernatant, salt fractionation, diafiltration, column chromatography and buffer exchanged into 1×PBS, pH 7.2. The HPV16 and HPV18 L1 antigens are recombinant proteins expressed and purified from Pichia pastoris cells. The method of production of recombinant HPV proteins and HbsAg-HPV16 L2 is previously described in WO2010/001409. Addition of other adjuvants further enhanced the potency of the vaccine preparation. Addition of polymorphic forms of inulin, particularly the gamma inulin enhanced the potency of the vaccines. Gamma inulin comprises particles with a molecular weight of above 8000 daltons and is virtually insoluble in water at 37° C. The high molecular weight inulin Orafti®HPX was obtained from Beneo Orafti, Belgium. Gamma inulin fractions were prepared by the methods outlined in the prior art (U.S. Pat. No. 4,954,622; PCT/AU86/00311) and the preparation of algammulin was as per the methods described by Cooper and Steele, 1991. The gamma inulin and algammulin preparations at a concentration of 2 mg/ml were used in the vaccine formulations. The vaccine antigens were mixed with adjuvants for two hours at ambient temperature and used immediately for injections. Similar formulation was also tested with phosphate-citrate buffer of pH 6.8-7.2 with adverse no effect on stability. Adsorption of the vaccine antigens to alum was tested by centrifuging the formulation and supernatant was checked by SDS-PAGE for protein bands of expected size for different antigens. All the aforementioned antigens adsorbed efficiently to alum. The vaccine formulations were tested in mice for potency.

Example-5

Potency Testing of the Vaccine Formulations

[0046] Six Balb/c mice were used per group for testing different viral antigen combinations described in Example 4. The highest vaccine antigen concentration is described in Example 4. Four two-fold dilutions of the vaccine formulations were injected intramuscularly in 6-8 week old mice of 18-20 g body weight. The dilutions were made in 1×PBS (50 mM phosphate buffer, pH 7.2 containing 150 mM NaCl) and containing the appropriate amount of adjuvant in order to maintain a constant adjuvant concentration. 2-phenoxyethanol was used as a vaccine preservative. For control animals, equal volume of buffer containing the same quantity of adjuvant was injected without the viral antigens. A booster injection was given on day 14 after the administration of the first vaccine dose. Blood was collected from retro-orbital sinus 7 days after administration of the booster dose, serum separated, heat inactivated at 560 C for 30 minutes and stored frozen at -800 C until used for serological assays. For testing the potency of diphtheria toxin, guinea pigs were used as described below in Example 6.

Example-6

Determination of Antibody Titer by ELISA and by Toxin Neutralization Assay

[0047] For estimation of the antibody titer to HEV, and the HEV chimeric antigen with HPV16 L2, the HEV antibodies were estimated by indirect ELISA. About 1 μg of the 54 kD vaccine antigen was coated on 96-well plate in carbonate buffer, pH 9.6 and incubated overnight at 2-8° C. Similarly for estimation of antibody titer to HPV16 and HPV18 L1 antigens and the HPV16 L2 epitopes, 1 μg of the purified HPV16 L1 and HPV18 L1 and HPV16 L2 antigens respectively were coated in 96-well plates in carbonate buffer, pH 9.6 incubated overnight at 2-8° C. The rest of the procedure for the above HEV and HPV antigens are same as described below. After discarding the plate contents, the wells were blocked with 3% skimmed milk powder in phosphate buffered saline, pH 7.4. The plates were incubated at 37° C. for one hour and were washed with the washing buffer containing 0.05% Tween-20 in PBS (PBST) five times. Serial two fold dilutions of the test sera were added and the plates were incubated at 37° C. for one and half hours. The plates were washed eight times with the wash buffer. The mouse anti-IgG HRPO conjugate was added at 1:2500 dilution and incubated at 37° C. for one hour. The wells were washed five times with wash buffer and three times with PBS and the color developed by adding OPD (O-phenylenediamine, Sigma Aldrich, USA) and H₂O₂. The readings were taken 10 min after the addition of 1N sulfuric acid. Antibody titer as a measure of seroconversion in animals was estimated as the reciprocal of the serum dilution that is above that of control animal+3×standard deviation of the control value. Antibody titers to HbsAg were estimated using the Axsym Ausab kit (Abbot Laboratories) as per the kit protocol provided by the manufacturer. A titer of 10 mIU/mL was considered as the cut-off for seroconversion. The antibody concentrations were expressed as mIU/mL. Diptheria antitoxins were estimated by the toxin neutralization test (TNT) in guinea pigs. Six animals were used per test group, control group and for the reference standard group. The reference standards were obtained from NIBSC. The dilutions of the vaccine and the reference standard were injected subcutaneously into the guinea pig and the control group received equal volume of the vehicle containing aluminum hydroxide. After four weeks the vaccinated animals were challenged with 100 LD50 of the diphtheria toxin. The control group was challenged with 1 LD50 of the toxin. The animals were observed for mortality in the different dilution groups and scored against the reference standard group. The cut off for potency was 30 IU/dose. All the animals seroconverted for the diphtheria toxin. The tetanus toxoid potency was assayed in Balb/c mice. Six animals were included in each test, reference standard and the control group. Four two-fold serial dilutions of the TT were injected in a volume of 0.5 ml subcutaneously in each mouse. After four weeks the vaccinated animals (both the test vaccine and the reference standard groups) were challenged with 100 LD50 of tetanus toxin in a volume of 0.5 ml. Control group were challenged with 1/50 to 1/200 dilution of the tetanus toxin. The animals were observed for mortality. The potency of the results was expressed in IU/ml (Table 1). The cut off for potency is 60 IU/dose. All the animals that were concomitantly administered the vaccines seroconverted and no antigenic interference of the vaccines antigens or alum was observed. The potency of the acellular pertussis components were assayed by ELISA against the antibody titers elicited by the detoxified pertussis toxin using reference standard from NIBSC. Antibody titer against pertactin proteins were also determined

TABLE-US-00001 TABLE 1 Potency testing of concomitantly administered vaccine antigens antibody titer (average Method for Vaccine antigens Animals for testing % seroconversion of 6 animals) antibody assay HEV + HbsAg-HPVL2 Mice, Balb/c 100% Anti-HbsAg (as ELISA, (Axsym (or HEV-HPVL2)@ + Mice, Balb/c HbsAg-L2) = 32 mIU/ml Ausab, Abbot HPV16 L1 + HPV18 Guinea pigs Laboratories) L1 + Tdap Anti HEV = 128,000* in-house indirect Tdap components: (measures HEV ELISA Tetanus antibody to both HEV Diptheria and HEV-L2 antigens) Acellular pertussis Anti- in-house indirect antigens: HPV16L1 = 64,000* ELISA detoxified pertussis Anti- in-house indirect toxin HPV18L1 = 128,000* ELISA Pertactin Anti-HPV16 L2 = in-house indirect FHA 12,800* (measures L2 ELISA antibody to both HEV- L2 and/or HbsAg-L2 antigens. Tetanus antitoxin = 75 IU/ml Toxin neutralization test Diptheria antitoxin = Toxin 45 IU/ml neutralization test Detox pertussis in-house ELISA antitoxin = 12800* Anti-pertactin = 6400* in-house ELISA Anti-FHA not determined *Antibody titer was estimated as the reciprocal of the serum dilution that is above that of control animal + 3 × standard deviation of the control value. @administration of either of the HbsAg-L2 or HEV-L2 elicited immune response against L2 epitope without interference from other antigens.

REFERENCES

[0048] 1. Emerson U E, Purcell R H. (2007): in Fields Virology, eds Knipe D, Howley P (Lippincott Williams & Wilkins, Philadelphia), Vol 1, pp 3047-3058.

[0049] 2. Chandra V, Taneja S, Kalia M, Jameel S. (2008): Molecular biology and pathogenesis of hepatitis E virus. J. Biosci 33, 451-464.

[0050] 3. Guu T S, Liu Z, Ye Q, Mata D A, Li K, Yin C, Zhang J, Tao Y J. (2009): Structure of the hepatitis E virus-like particle suggests mechanisms for virus assembly and receptor binding. Proc Natl Acad Sci USA. 106, 12992-12997.

[0051] 4. Khuroo M S, Teli M R, Skidmore S, et al. (1981): Incidence and severity of viral hepatitis in pregnancy. Am J Med 70:252-255.

[0052] 5. Tsega E, Krawzyski K, Hansson L, et al. 1993: Hepatitis E virus infection in pregnancy in Ethiopia. Ethiop Med J 1993; 31:173-181.

[0053] 6. Lindemann M L M, Morales J G, Ferna'ndez-Barrado S, et al. (2010): Case report: fulminant hepatitis E in a woman taking oral contraceptive medication. Am J Trop Med Hyg, 82, 12-15.

[0054] 7. Schofield F D, Tucker V M, Westbrook G R. (1961): Neonatal tetanus in New Guinea. Effect of active immunization in pregnancy. Br Med J 2, 785-789.

[0055] 8. Nanda S. K, Yalcinkaya K, Panigrahi A. K, Acharya S. K, Jameel S and Panda S. K. (1994): "Etiological role of hepatitis E virus in sporadic fulminant hepatitis," Journal of Medical Virology, 42, 133-137.

[0056] 9. Beniwal M, Kumar A, Kar P, (2003): Prevalence and severity of acute viral hepatitis and fulminant hepatitis during pregnancy: a prospective study from North India. Indian J Med Microbiol. 21, 184-185.

[0057] 10. Kumar A, Beniwal B, Kar P, et al. (2004): Hepatitis E in pregnancy. Int J Gynaecol Obstet. 85, 240-244.

[0058] 11. Khuroo M S, Salimi K, Jameel S. (1995): Vertical transmission of hepatitis E virus. Lancet. 345, 1025-1026.

[0059] 12. Amini-Bavil-Olyaee S, Trautwein C, Tacke F. (2009): Hepatitis E Vaccine: Current Status and Future Prospects. Future Virology. 4, 143-154.

[0060] 13. Zhu et al., (2010): Efficacy and safety of a recombinant hepatitis E vaccine in healthy adults: a large-scale, randomised, double-blind placebo-controlled, phase 3 trial. The Lancet, 376, 895-902.

[0061] 14. Mushahwar I K. (2008): Hepatitis E virus: molecular virology, clinical features, diagnosis, transmission, epidemiology, and prevention. J Med Virol. 80, 646-658.

Sequence CWU 1

1

231660PRTArtificial SequenceHEV ORF2 1Met Arg Pro Arg Pro Ile Leu Leu Leu Phe Leu Met Phe Leu Pro Met 1 5 10 15 Leu Pro Ala Pro Pro Pro Gly Gln Pro Ser Gly Arg Arg Arg Gly Arg 20 25 30 Arg Ser Gly Gly Ser Gly Gly Gly Phe Trp Gly Asp Arg Val Asp Ser 35 40 45 Gln Pro Phe Ala Ile Pro Tyr Ile His Pro Thr Asn Pro Phe Ala Pro 50 55 60 Asp Val Thr Ala Ala Ala Gly Ala Gly Pro Arg Val Arg Gln Pro Ala 65 70 75 80 Arg Pro Leu Gly Ser Ala Trp Arg Asp Gln Ala Gln Arg Pro Ala Ala 85 90 95 Ala Ser Arg Arg Arg Pro Thr Thr Ala Gly Ala Ala Pro Leu Thr Ala 100 105 110 Val Ala Pro Ala His Asp Thr Pro Pro Val Pro Asp Val Asp Ser Arg 115 120 125 Gly Ala Ile Leu Arg Arg Gln Tyr Asn Leu Ser Thr Ser Pro Leu Thr 130 135 140 Ser Ser Val Ala Thr Gly Thr Asn Leu Val Leu Tyr Ala Ala Pro Leu 145 150 155 160 Ser Pro Leu Leu Pro Leu Gln Asp Gly Thr Asn Thr His Ile Met Ala 165 170 175 Thr Glu Ala Ser Asn Tyr Ala Gln Tyr Arg Val Ala Arg Ala Thr Ile 180 185 190 Arg Tyr Arg Pro Leu Val Pro Asn Ala Val Gly Gly Tyr Ala Ile Ser 195 200 205 Ile Ser Phe Trp Pro Gln Thr Thr Thr Thr Pro Thr Ser Val Asp Met 210 215 220 Asn Ser Ile Thr Ser Thr Asp Val Arg Ile Leu Val Gln Pro Gly Ile 225 230 235 240 Ala Ser Glu Leu Val Ile Pro Ser Glu Arg Leu His Tyr Arg Asn Gln 245 250 255 Gly Trp Arg Ser Val Glu Thr Ser Gly Val Ala Glu Glu Glu Ala Thr 260 265 270 Ser Gly Leu Val Met Leu Cys Ile His Gly Ser Pro Val Asn Ser Tyr 275 280 285 Thr Asn Thr Pro Tyr Thr Gly Ala Leu Gly Leu Leu Asp Phe Ala Leu 290 295 300 Glu Leu Glu Phe Arg Asn Leu Thr Pro Gly Asn Thr Asn Thr Arg Val 305 310 315 320 Ser Arg Tyr Ser Ser Thr Ala Arg His Arg Leu Arg Arg Gly Ala Asp 325 330 335 Gly Thr Ala Glu Leu Thr Thr Thr Ala Ala Thr Arg Phe Met Lys Asp 340 345 350 Leu Tyr Phe Thr Ser Thr Asn Gly Val Gly Glu Ile Gly Arg Gly Ile 355 360 365 Ala Leu Thr Leu Phe Asn Leu Ala Asp Thr Leu Leu Gly Gly Leu Pro 370 375 380 Thr Glu Leu Ile Ser Ser Ala Gly Gly Gln Leu Phe Tyr Ser Arg Pro 385 390 395 400 Val Val Ser Ala Asn Gly Glu Pro Thr Val Lys Leu Tyr Thr Ser Val 405 410 415 Glu Asn Ala Gln Gln Asp Lys Gly Ile Ala Ile Pro His Asp Ile Asp 420 425 430 Leu Gly Glu Ser Arg Val Val Ile Gln Asp Tyr Asp Asn Gln His Glu 435 440 445 Gln Asp Arg Pro Thr Pro Ser Pro Ala Pro Ser Arg Pro Phe Ser Val 450 455 460 Leu Arg Ala Asn Asp Val Leu Trp Leu Ser Leu Thr Ala Ala Glu Tyr 465 470 475 480 Asp Gln Ser Thr Tyr Gly Ser Ser Thr Gly Pro Val Tyr Val Ser Asp 485 490 495 Ser Val Thr Leu Val Asn Val Ala Thr Gly Ala Gln Ala Val Ala Arg 500 505 510 Ser Leu Asp Trp Thr Lys Val Thr Leu Asp Gly Arg Pro Leu Ser Thr 515 520 525 Ile Gln Gln Tyr Ser Lys Thr Phe Phe Val Leu Pro Leu Arg Gly Lys 530 535 540 Leu Ser Phe Trp Glu Ala Gly Thr Thr Lys Ala Gly Tyr Pro Tyr Asn 545 550 555 560 Tyr Asn Thr Thr Ala Ser Asp Gln Leu Leu Val Glu Asn Ala Ala Gly 565 570 575 His Arg Val Ala Ile Ser Thr Tyr Thr Thr Ser Leu Gly Ala Gly Pro 580 585 590 Val Ser Ile Ser Ala Val Ala Val Leu Ala Pro His Ser Ala Leu Ala 595 600 605 Leu Leu Glu Asp Thr Leu Asp Tyr Pro Ala Arg Ala His Thr Phe Asp 610 615 620 Asp Phe Cys Pro Glu Cys Arg Pro Leu Gly Leu Gln Gly Cys Ala Phe 625 630 635 640 Gln Ser Thr Val Ala Glu Leu Gln Arg Leu Lys Met Lys Val Gly Lys 645 650 655 Thr Arg Glu Leu 660 2473PRTArtificial SequenceHPV16 L2 2Met Arg His Lys Arg Ser Ala Lys Arg Thr Lys Arg Ala Ser Ala Thr 1 5 10 15 Gln Leu Tyr Lys Thr Cys Lys Gln Ala Gly Thr Cys Pro Pro Asp Ile 20 25 30 Ile Pro Lys Val Glu Gly Lys Thr Ile Ala Asp Gln Ile Leu Gln Tyr 35 40 45 Gly Ser Met Gly Val Phe Phe Gly Gly Leu Gly Ile Gly Thr Gly Ser 50 55 60 Gly Thr Gly Gly Arg Thr Gly Tyr Ile Pro Leu Gly Thr Arg Pro Pro 65 70 75 80 Thr Ala Thr Asp Thr Leu Ala Pro Val Arg Pro Pro Leu Thr Val Asp 85 90 95 Pro Val Gly Pro Ser Asp Pro Ser Ile Val Ser Leu Val Glu Glu Thr 100 105 110 Ser Phe Ile Asp Ala Gly Ala Pro Thr Pro Val Pro Ser Ile Pro Pro 115 120 125 Asp Val Ser Gly Phe Ser Ile Thr Thr Ser Thr Asp Thr Thr Pro Ala 130 135 140 Ile Leu Asp Ile Asn Asn Thr Val Thr Thr Val Thr Thr His Asn Asn 145 150 155 160 Pro Thr Phe Thr Asp Pro Ser Val Leu Gln Pro Pro Thr Pro Ala Glu 165 170 175 Thr Gly Gly His Phe Thr Leu Ser Ser Ser Thr Ile Ser Thr His Asn 180 185 190 Tyr Glu Glu Ile Pro Met Asp Thr Phe Ile Val Ser Thr Asn Pro Asn 195 200 205 Thr Val Thr Ser Ser Thr Pro Ile Pro Gly Ser Arg Pro Val Ala Arg 210 215 220 Leu Gly Leu Tyr Ser Arg Thr Thr Gln Gln Val Lys Val Val Asp Pro 225 230 235 240 Ala Phe Val Thr Thr Pro Thr Lys Leu Ile Thr Tyr Asp Asn Pro Ala 245 250 255 Tyr Glu Gly Ile Asp Val Asp Asn Thr Leu Tyr Phe Ser Ser Asn Asp 260 265 270 Asn Ser Ile Asn Ile Ala Pro Asp Pro Asp Phe Leu Asp Ile Val Ala 275 280 285 Leu His Arg Pro Ala Leu Thr Ser Arg Arg Thr Gly Ile Arg Tyr Ser 290 295 300 Arg Ile Gly Asn Lys Gln Thr Leu Arg Thr Arg Ser Gly Lys Ser Ile 305 310 315 320 Gly Ala Lys Val His Tyr Tyr Tyr Asp Phe Ser Thr Ile Asp Pro Ala 325 330 335 Glu Glu Ile Glu Leu Gln Thr Ile Thr Pro Ser Thr Tyr Thr Thr Thr 340 345 350 Ser His Ala Ala Ser Pro Thr Ser Ile Asn Asn Gly Leu Tyr Asp Ile 355 360 365 Tyr Ala Asp Asp Phe Ile Thr Asp Thr Ser Thr Thr Pro Val Pro Ser 370 375 380 Val Pro Ser Thr Ser Leu Ser Gly Tyr Ile Pro Ala Asn Thr Thr Ile 385 390 395 400 Pro Phe Gly Gly Ala Tyr Asn Ile Pro Leu Val Ser Gly Pro Asp Ile 405 410 415 Pro Ile Asn Ile Thr Asp Gln Ala Pro Ser Leu Ile Pro Ile Val Pro 420 425 430 Gly Ser Pro Gln Tyr Thr Ile Ile Ala Asp Ala Gly Asp Phe Tyr Leu 435 440 445 His Pro Ser Tyr Tyr Met Leu Arg Lys Arg Arg Lys Arg Leu Pro Tyr 450 455 460 Phe Phe Ser Asp Val Ser Leu Ala Ala 465 470 31494DNAArtificial SequenceHEV ORF2 DNA 3atggccgttg cacctgctca tgatactcct ccagttccag atgttgattc tagaggtgct 60atcttgagaa gacaatacaa ccttagtacc tctcctttga cttcttccgt tgctactggt 120acaaatcttg tcttgtacgc agctccactt tcacctcttt tgccattgca agacggaacc 180aacactcaca tcatggctac agaagccagt aattatgctc agtacagagt tgccagagca 240actattagat atagaccttt ggttccaaac gcagtcggag gttacgctat ttccatctca 300ttctggccac aaaccactac aacccctact tctgttgata tgaactctat cacatcaacc 360gacgttagaa ttttggtcca accaggtatc gcttctgagc ttgttattcc ttccgaaaga 420ttgcattata gaaaccaggg ttggagatcc gttgaaacat caggagtcgc agaagaggaa 480gctacctctg gtcttgttat gttgtgtatt cacggaagtc cagtcaactc ttatactaat 540acaccttaca ctggagcatt gggtcttttg gattttgctc ttgagttgga gtttagaaat 600ttgactcctg gtaacaccaa cactagagtt tctagatact caagtactgc tagacataga 660ttgagaagag gagccgatgg tactgcagag ttgactacaa ccgccgcaac aagattcatg 720aaagacttgt acttcacatc caccaacgga gttggtgaaa ttggaagagg tatcgccctt 780acattgttta atttggcaga tacccttttg ggaggtcttc caactgagtt gatttcttcc 840gctggaggtc aattgttcta ttctagacca gttgtctccg ctaacggaga gcctacagtt 900aaattgtaca cctcagtcga aaatgctcaa caggataagg gtattgccat ccctcatgat 960atcgacttgg gagagtctag agttgtcatt caggattacg acaaccaaca cgaacaggac 1020agacctactc catcccctgc cccatctaga ccattttctg ttttgagagc aaatgatgtc 1080ctttggttgt cacttactgc tgccgaatat gaccaaagta cttacggttc aagtacagga 1140cctgtttatg tcagtgattc tgttaccttg gttaacgtcg ctactggtgc tcaggccgtt 1200gcaagatcct tggattggac taaggtcaca cttgacggaa gaccattgtc aacaattcaa 1260cagtacagta agaccttttt cgttttgcct cttcgtggta aattgtcttt ctgggaagcc 1320ggtactacaa aggcaggata cccatataac tacaatacca ctgcttccga tcaacttttg 1380gttgagaatg cagctggtca cagagtcgct atctcaactt atacaaccag tttgggagcc 1440ggtccagttt ccatttcagc tgttgccgtc cttgctcctc attctgcatt ggct 14944498PRTArtificial Sequence112-608 AAHEV ORF2 4Met Ala Val Ala Pro Ala His Asp Thr Pro Pro Val Pro Asp Val Asp 1 5 10 15 Ser Arg Gly Ala Ile Leu Arg Arg Gln Tyr Asn Leu Ser Thr Ser Pro 20 25 30 Leu Thr Ser Ser Val Ala Thr Gly Thr Asn Leu Val Leu Tyr Ala Ala 35 40 45 Pro Leu Ser Pro Leu Leu Pro Leu Gln Asp Gly Thr Asn Thr His Ile 50 55 60 Met Ala Thr Glu Ala Ser Asn Tyr Ala Gln Tyr Arg Val Ala Arg Ala 65 70 75 80 Thr Ile Arg Tyr Arg Pro Leu Val Pro Asn Ala Val Gly Gly Tyr Ala 85 90 95 Ile Ser Ile Ser Phe Trp Pro Gln Thr Thr Thr Thr Pro Thr Ser Val 100 105 110 Asp Met Asn Ser Ile Thr Ser Thr Asp Val Arg Ile Leu Val Gln Pro 115 120 125 Gly Ile Ala Ser Glu Leu Val Ile Pro Ser Glu Arg Leu His Tyr Arg 130 135 140 Asn Gln Gly Trp Arg Ser Val Glu Thr Ser Gly Val Ala Glu Glu Glu 145 150 155 160 Ala Thr Ser Gly Leu Val Met Leu Cys Ile His Gly Ser Pro Val Asn 165 170 175 Ser Tyr Thr Asn Thr Pro Tyr Thr Gly Ala Leu Gly Leu Leu Asp Phe 180 185 190 Ala Leu Glu Leu Glu Phe Arg Asn Leu Thr Pro Gly Asn Thr Asn Thr 195 200 205 Arg Val Ser Arg Tyr Ser Ser Thr Ala Arg His Arg Leu Arg Arg Gly 210 215 220 Ala Asp Gly Thr Ala Glu Leu Thr Thr Thr Ala Ala Thr Arg Phe Met 225 230 235 240 Lys Asp Leu Tyr Phe Thr Ser Thr Asn Gly Val Gly Glu Ile Gly Arg 245 250 255 Gly Ile Ala Leu Thr Leu Phe Asn Leu Ala Asp Thr Leu Leu Gly Gly 260 265 270 Leu Pro Thr Glu Leu Ile Ser Ser Ala Gly Gly Gln Leu Phe Tyr Ser 275 280 285 Arg Pro Val Val Ser Ala Asn Gly Glu Pro Thr Val Lys Leu Tyr Thr 290 295 300 Ser Val Glu Asn Ala Gln Gln Asp Lys Gly Ile Ala Ile Pro His Asp 305 310 315 320 Ile Asp Leu Gly Glu Ser Arg Val Val Ile Gln Asp Tyr Asp Asn Gln 325 330 335 His Glu Gln Asp Arg Pro Thr Pro Ser Pro Ala Pro Ser Arg Pro Phe 340 345 350 Ser Val Leu Arg Ala Asn Asp Val Leu Trp Leu Ser Leu Thr Ala Ala 355 360 365 Glu Tyr Asp Gln Ser Thr Tyr Gly Ser Ser Thr Gly Pro Val Tyr Val 370 375 380 Ser Asp Ser Val Thr Leu Val Asn Val Ala Thr Gly Ala Gln Ala Val 385 390 395 400 Ala Arg Ser Leu Asp Trp Thr Lys Val Thr Leu Asp Gly Arg Pro Leu 405 410 415 Ser Thr Ile Gln Gln Tyr Ser Lys Thr Phe Phe Val Leu Pro Leu Arg 420 425 430 Gly Lys Leu Ser Phe Trp Glu Ala Gly Thr Thr Lys Ala Gly Tyr Pro 435 440 445 Tyr Asn Tyr Asn Thr Thr Ala Ser Asp Gln Leu Leu Val Glu Asn Ala 450 455 460 Ala Gly His Arg Val Ala Ile Ser Thr Tyr Thr Thr Ser Leu Gly Ala 465 470 475 480 Gly Pro Val Ser Ile Ser Ala Val Ala Val Leu Ala Pro His Ser Ala 485 490 495 Leu Ala 51572DNAArtificial SequenceHEV-HPV16L2 chimeric gene (1572 bp) DNA 5atgtctgcaa ctcagttgta taaaacttgc aagcaagctg gtacttgccc accagacatt 60atcccaaagg ttgaaggatc cgccgttgca cctgctcatg atactcctcc agttccagat 120gttgattcta gaggtgctat cttgagaaga caatacaacc ttagtacctc tcctttgact 180tcttccgttg ctactggtac aaatcttgtc ttgtacgcag ctccactttc acctcttttg 240ccattgcaag acggaaccaa cactcacatc atggctacag aagccagtaa ttatgctcag 300tacagagttg ccagagcaac tattagatat agacctttgg ttccaaacgc agtcggaggt 360tacgctattt ccatctcatt ctggccacaa accactacaa cccctacttc tgttgatatg 420aactctatca catcaaccga cgttagaatt ttggtccaac caggtatcgc ttctgagctt 480gttattcctt ccgaaagatt gcattataga aaccagggtt ggagatccgt tgaaacatca 540ggagtcgcag aagaggaagc tacctctggt cttgttatgt tgtgtattca cggaagtcca 600gtcaactctt atactaatac accttacact ggagcattgg gtcttttgga ttttgctctt 660gagttggagt ttagaaattt gactcctggt aacaccaaca ctagagtttc tagatactca 720agtactgcta gacatagatt gagaagagga gccgatggta ctgcagagtt gactacaacc 780gccgcaacaa gattcatgaa agacttgtac ttcacatcca ccaacggagt tggtgaaatt 840ggaagaggta tcgcccttac attgtttaat ttggcagata cccttttggg aggtcttcca 900actgagttga tttcttccgc tggaggtcaa ttgttctatt ctagaccagt tgtctccgct 960aacggagagc ctacagttaa attgtacacc tcagtcgaaa atgctcaaca ggataagggt 1020attgccatcc ctcatgatat cgacttggga gagtctagag ttgtcattca ggattacgac 1080aaccaacacg aacaggacag acctactcca tcccctgccc catctagacc attttctgtt 1140ttgagagcaa atgatgtcct ttggttgtca cttactgctg ccgaatatga ccaaagtact 1200tacggttcaa gtacaggacc tgtttatgtc agtgattctg ttaccttggt taacgtcgct 1260actggtgctc aggccgttgc aagatccttg gattggacta aggtcacact tgacggaaga 1320ccattgtcaa caattcaaca gtacagtaag acctttttcg ttttgcctct tcgtggtaaa 1380ttgtctttct gggaagccgg tactacaaag gcaggatacc catataacta caataccact 1440gcttccgatc aacttttggt tgagaatgca gctggtcaca gagtcgctat ctcaacttat 1500acaaccagtt tgggagccgg tccagtttcc atttcagctg ttgccgtcct tgctcctcat 1560tctgcattgg ct 15726524PRTArtificial SequenceHEV-HPV16 L2 chimera (524 AA) 6Met Ser Ala Thr Gln Leu Tyr Lys Thr Cys Lys Gln Ala Gly Thr Cys 1 5 10 15 Pro Pro Asp Ile Ile Pro Lys Val Glu Gly Ser Ala Val Ala Pro Ala 20 25 30 His Asp Thr Pro Pro Val Pro Asp Val Asp Ser Arg Gly Ala Ile Leu 35 40 45 Arg Arg Gln Tyr Asn Leu Ser Thr Ser Pro Leu Thr Ser Ser Val Ala 50 55 60 Thr Gly Thr Asn Leu Val Leu Tyr Ala Ala Pro Leu Ser Pro Leu Leu 65 70 75 80 Pro Leu Gln Asp Gly Thr Asn Thr His Ile Met Ala Thr Glu Ala Ser 85 90 95 Asn Tyr Ala Gln Tyr Arg Val Ala Arg Ala Thr Ile Arg Tyr Arg Pro 100 105 110 Leu Val Pro Asn Ala Val Gly Gly Tyr Ala Ile Ser Ile Ser Phe Trp 115 120 125 Pro Gln Thr Thr Thr Thr Pro Thr Ser Val Asp Met Asn Ser Ile Thr 130 135 140 Ser Thr Asp Val Arg Ile Leu Val Gln Pro Gly Ile Ala Ser Glu Leu 145 150 155

160 Val Ile Pro Ser Glu Arg Leu His Tyr Arg Asn Gln Gly Trp Arg Ser 165 170 175 Val Glu Thr Ser Gly Val Ala Glu Glu Glu Ala Thr Ser Gly Leu Val 180 185 190 Met Leu Cys Ile His Gly Ser Pro Val Asn Ser Tyr Thr Asn Thr Pro 195 200 205 Tyr Thr Gly Ala Leu Gly Leu Leu Asp Phe Ala Leu Glu Leu Glu Phe 210 215 220 Arg Asn Leu Thr Pro Gly Asn Thr Asn Thr Arg Val Ser Arg Tyr Ser 225 230 235 240 Ser Thr Ala Arg His Arg Leu Arg Arg Gly Ala Asp Gly Thr Ala Glu 245 250 255 Leu Thr Thr Thr Ala Ala Thr Arg Phe Met Lys Asp Leu Tyr Phe Thr 260 265 270 Ser Thr Asn Gly Val Gly Glu Ile Gly Arg Gly Ile Ala Leu Thr Leu 275 280 285 Phe Asn Leu Ala Asp Thr Leu Leu Gly Gly Leu Pro Thr Glu Leu Ile 290 295 300 Ser Ser Ala Gly Gly Gln Leu Phe Tyr Ser Arg Pro Val Val Ser Ala 305 310 315 320 Asn Gly Glu Pro Thr Val Lys Leu Tyr Thr Ser Val Glu Asn Ala Gln 325 330 335 Gln Asp Lys Gly Ile Ala Ile Pro His Asp Ile Asp Leu Gly Glu Ser 340 345 350 Arg Val Val Ile Gln Asp Tyr Asp Asn Gln His Glu Gln Asp Arg Pro 355 360 365 Thr Pro Ser Pro Ala Pro Ser Arg Pro Phe Ser Val Leu Arg Ala Asn 370 375 380 Asp Val Leu Trp Leu Ser Leu Thr Ala Ala Glu Tyr Asp Gln Ser Thr 385 390 395 400 Tyr Gly Ser Ser Thr Gly Pro Val Tyr Val Ser Asp Ser Val Thr Leu 405 410 415 Val Asn Val Ala Thr Gly Ala Gln Ala Val Ala Arg Ser Leu Asp Trp 420 425 430 Thr Lys Val Thr Leu Asp Gly Arg Pro Leu Ser Thr Ile Gln Gln Tyr 435 440 445 Ser Lys Thr Phe Phe Val Leu Pro Leu Arg Gly Lys Leu Ser Phe Trp 450 455 460 Glu Ala Gly Thr Thr Lys Ala Gly Tyr Pro Tyr Asn Tyr Asn Thr Thr 465 470 475 480 Ala Ser Asp Gln Leu Leu Val Glu Asn Ala Ala Gly His Arg Val Ala 485 490 495 Ile Ser Thr Tyr Thr Thr Ser Leu Gly Ala Gly Pro Val Ser Ile Ser 500 505 510 Ala Val Ala Val Leu Ala Pro His Ser Ala Leu Ala 515 520 71572DNAArtificial SequenceHEV-HPV16L2 chimeric gene (1572 bp) 7atggccgttg cacctgctca tgatactcct ccagttccag atgttgattc tagaggtgct 60atcttgagaa gacaatacaa ccttagtacc tctcctttga cttcttccgt tgctactggt 120acaaatcttg tcttgtacgc agctccactt tcacctcttt tgccattgca agacggaacc 180aacactcaca tcatggctac agaagccagt aattatgctc agtacagagt tgccagagca 240actattagat atagaccttt ggttccaaac gcagtcggag gttacgctat ttccatctca 300ttctggccac aaaccactac aacccctact tctgttgata tgaactctat cacatcaacc 360gacgttagaa ttttggtcca accaggtatc gcttctgagc ttgttattcc ttccgaaaga 420ttgcattata gaaaccaggg ttggagatcc gttgaaacat caggagtcgc agaagaggaa 480gctacctctg gtcttgttat gttgtgtatt cacggaagtc cagtcaactc ttatactaat 540acaccttaca ctggagcatt gggtcttttg gattttgctc ttgagttgga gtttagaaat 600ttgactcctg gtaacaccaa cactagagtt tctagatact caagtactgc tagacataga 660ttgagaagag gagccgatgg tactgcagag ttgactacaa ccgccgcaac aagattcatg 720aaagacttgt acttcacatc caccaacgga gttggtgaaa ttggaagagg tatcgccctt 780acattgttta atttggcaga tacccttttg ggaggtcttc caactgagtt gatttcttcc 840gctggaggtc aattgttcta ttctagacca gttgtctccg ctaacggaga gcctacagtt 900aaattgtaca cctcagtcga aaatgctcaa caggataagg gtattgccat ccctcatgat 960atcgacttgg gagagtctag agttgtcatt caggattacg acaaccaaca cgaacaggac 1020agacctactc catcccctgc cccatctaga ccattttctg ttttgagagc aaatgatgtc 1080ctttggttgt cacttactgc tgccgaatat gaccaaagta cttacggttc aagtacagga 1140cctgtttatg tcagtgattc tgttaccttg gttaacgtcg ctactggtgc tcaggccgtt 1200gcaagatcct tggattggac taaggtcaca cttgacggaa gaccattgtc aacaattcaa 1260cagtacagta agaccttttt cgttttgcct cttcgtggta aattgtcttt ctgggaagcc 1320ggtactacaa aggcaggata cccatataac tacaatacca ctgcttccga tcaacttttg 1380gttgagaatg cagctggtca cagagtcgct atctcaactt atacaaccag tttgggagcc 1440ggtccagttt ccatttcagc tgttgccgtc cttgctcctc attctgcatt ggctggatct 1500gcaactcagt tgtataaaac ttgcaagcaa gctggtactt gcccaccaga cattatccca 1560aaggttgaag ga 15728524PRTArtificial SequenceHEV-HPV16L2 chimeric protein (524 AA) 8Met Ala Val Ala Pro Ala His Asp Thr Pro Pro Val Pro Asp Val Asp 1 5 10 15 Ser Arg Gly Ala Ile Leu Arg Arg Gln Tyr Asn Leu Ser Thr Ser Pro 20 25 30 Leu Thr Ser Ser Val Ala Thr Gly Thr Asn Leu Val Leu Tyr Ala Ala 35 40 45 Pro Leu Ser Pro Leu Leu Pro Leu Gln Asp Gly Thr Asn Thr His Ile 50 55 60 Met Ala Thr Glu Ala Ser Asn Tyr Ala Gln Tyr Arg Val Ala Arg Ala 65 70 75 80 Thr Ile Arg Tyr Arg Pro Leu Val Pro Asn Ala Val Gly Gly Tyr Ala 85 90 95 Ile Ser Ile Ser Phe Trp Pro Gln Thr Thr Thr Thr Pro Thr Ser Val 100 105 110 Asp Met Asn Ser Ile Thr Ser Thr Asp Val Arg Ile Leu Val Gln Pro 115 120 125 Gly Ile Ala Ser Glu Leu Val Ile Pro Ser Glu Arg Leu His Tyr Arg 130 135 140 Asn Gln Gly Trp Arg Ser Val Glu Thr Ser Gly Val Ala Glu Glu Glu 145 150 155 160 Ala Thr Ser Gly Leu Val Met Leu Cys Ile His Gly Ser Pro Val Asn 165 170 175 Ser Tyr Thr Asn Thr Pro Tyr Thr Gly Ala Leu Gly Leu Leu Asp Phe 180 185 190 Ala Leu Glu Leu Glu Phe Arg Asn Leu Thr Pro Gly Asn Thr Asn Thr 195 200 205 Arg Val Ser Arg Tyr Ser Ser Thr Ala Arg His Arg Leu Arg Arg Gly 210 215 220 Ala Asp Gly Thr Ala Glu Leu Thr Thr Thr Ala Ala Thr Arg Phe Met 225 230 235 240 Lys Asp Leu Tyr Phe Thr Ser Thr Asn Gly Val Gly Glu Ile Gly Arg 245 250 255 Gly Ile Ala Leu Thr Leu Phe Asn Leu Ala Asp Thr Leu Leu Gly Gly 260 265 270 Leu Pro Thr Glu Leu Ile Ser Ser Ala Gly Gly Gln Leu Phe Tyr Ser 275 280 285 Arg Pro Val Val Ser Ala Asn Gly Glu Pro Thr Val Lys Leu Tyr Thr 290 295 300 Ser Val Glu Asn Ala Gln Gln Asp Lys Gly Ile Ala Ile Pro His Asp 305 310 315 320 Ile Asp Leu Gly Glu Ser Arg Val Val Ile Gln Asp Tyr Asp Asn Gln 325 330 335 His Glu Gln Asp Arg Pro Thr Pro Ser Pro Ala Pro Ser Arg Pro Phe 340 345 350 Ser Val Leu Arg Ala Asn Asp Val Leu Trp Leu Ser Leu Thr Ala Ala 355 360 365 Glu Tyr Asp Gln Ser Thr Tyr Gly Ser Ser Thr Gly Pro Val Tyr Val 370 375 380 Ser Asp Ser Val Thr Leu Val Asn Val Ala Thr Gly Ala Gln Ala Val 385 390 395 400 Ala Arg Ser Leu Asp Trp Thr Lys Val Thr Leu Asp Gly Arg Pro Leu 405 410 415 Ser Thr Ile Gln Gln Tyr Ser Lys Thr Phe Phe Val Leu Pro Leu Arg 420 425 430 Gly Lys Leu Ser Phe Trp Glu Ala Gly Thr Thr Lys Ala Gly Tyr Pro 435 440 445 Tyr Asn Tyr Asn Thr Thr Ala Ser Asp Gln Leu Leu Val Glu Asn Ala 450 455 460 Ala Gly His Arg Val Ala Ile Ser Thr Tyr Thr Thr Ser Leu Gly Ala 465 470 475 480 Gly Pro Val Ser Ile Ser Ala Val Ala Val Leu Ala Pro His Ser Ala 485 490 495 Leu Ala Gly Ser Ala Thr Gln Leu Tyr Lys Thr Cys Lys Gln Ala Gly 500 505 510 Thr Cys Pro Pro Asp Ile Ile Pro Lys Val Glu Gly 515 520 91539DNAArtificial SequenceHEV-HPV16L2 chimeric gene (1539 bp) 9atggccgttg cacctgctca tgatactcct ccagttccag atgttgattc tagaggtgct 60atcttgagaa gacaatacaa ccttagtacc tctcctttga cttcttccgt tgctactggt 120acaaatcttg tcttgtacgc agctccactt tcacctcttt tgccattgca agacggaacc 180aacactcaca tcatggctac agaagccagt aattatgctc agtacagagt tgccagagca 240actattagat atagaccttt ggttccaaac gcagtcggag gttacgctat ttccatctca 300ttctggccac aaaccactac aacccctact tctgttgata tgaactctat cacatcaacc 360gacgttagaa ttttggtcca accaggtatc gcttctgagc ttgttattcc ttccgaaaga 420ttgcattata gaaaccaggg ttggagatcc gttgaaacat caggagtcgc agaagaggaa 480gctacctctg gtcttgttat gttgtgtatt cacggaagtc cagtcaactc ttatactaat 540acaccttaca ctggagcatt gggtcttttg gattttgctc ttgagttgga gtttagaaat 600ttgactcctg gtaacaccaa cactagagtt tctagatact caagtactgc tagacataga 660ttgagaagag gagccgatgg tactgcagag ttgactacaa ccgccgcaac aagattcatg 720aaagacttgt acttcacatc caccaacgga gttggtgaaa ttggaagagg tatcgccctt 780acattgttta atttggcaga tacccttttg ggaggtcttc caactgagtt gatttcttcc 840gctggaggtc aattgttcta ttctagacca gttgtctccg ctaacggaga gcctacagtt 900aaattgtaca cctcagtcga aaatgctcaa caggataagg gtattgccat ccctcatgat 960atcgacttgg gagagtctag agttgtcatt caggattacg acaaccaaca cgaacaggac 1020agacctactc catcccctgc cccatctaga ccattttctg ttttgagagc aaatgatgtc 1080ctttggttgt cacttactgc tgccgaatat gaccaaagta cttacggttc aagtacagga 1140cctgtttatg tcagtgattc tgttaccttg gttaacgtcg ctactggtgc tcaggccgtt 1200gcaagatcct tggattggac taaggtcaca cttgacggaa gaccattgtc aacaattcaa 1260cagtacagta agaccttttt cgttttgcct cttcgtggta aattgtcttt ctgggaagcc 1320ggtactacaa aggcaggata cccatataac tacaatacca ctgcttccga tcaacttttg 1380gttgagaatg cagctggtca cagagtcgct atctcaactt atacaaccag tttgggagcc 1440ggtccagttt ccatttcagc tgttgccgtc cttgctcctc attctgcatt ggctggatcc 1500ttggttgaag aaacctcctt tattgacgct ggtgctcca 153910513PRTArtificial SequenceHEV-HPV16L2 chimeric protein (513 AA) 10Met Ala Val Ala Pro Ala His Asp Thr Pro Pro Val Pro Asp Val Asp 1 5 10 15 Ser Arg Gly Ala Ile Leu Arg Arg Gln Tyr Asn Leu Ser Thr Ser Pro 20 25 30 Leu Thr Ser Ser Val Ala Thr Gly Thr Asn Leu Val Leu Tyr Ala Ala 35 40 45 Pro Leu Ser Pro Leu Leu Pro Leu Gln Asp Gly Thr Asn Thr His Ile 50 55 60 Met Ala Thr Glu Ala Ser Asn Tyr Ala Gln Tyr Arg Val Ala Arg Ala 65 70 75 80 Thr Ile Arg Tyr Arg Pro Leu Val Pro Asn Ala Val Gly Gly Tyr Ala 85 90 95 Ile Ser Ile Ser Phe Trp Pro Gln Thr Thr Thr Thr Pro Thr Ser Val 100 105 110 Asp Met Asn Ser Ile Thr Ser Thr Asp Val Arg Ile Leu Val Gln Pro 115 120 125 Gly Ile Ala Ser Glu Leu Val Ile Pro Ser Glu Arg Leu His Tyr Arg 130 135 140 Asn Gln Gly Trp Arg Ser Val Glu Thr Ser Gly Val Ala Glu Glu Glu 145 150 155 160 Ala Thr Ser Gly Leu Val Met Leu Cys Ile His Gly Ser Pro Val Asn 165 170 175 Ser Tyr Thr Asn Thr Pro Tyr Thr Gly Ala Leu Gly Leu Leu Asp Phe 180 185 190 Ala Leu Glu Leu Glu Phe Arg Asn Leu Thr Pro Gly Asn Thr Asn Thr 195 200 205 Arg Val Ser Arg Tyr Ser Ser Thr Ala Arg His Arg Leu Arg Arg Gly 210 215 220 Ala Asp Gly Thr Ala Glu Leu Thr Thr Thr Ala Ala Thr Arg Phe Met 225 230 235 240 Lys Asp Leu Tyr Phe Thr Ser Thr Asn Gly Val Gly Glu Ile Gly Arg 245 250 255 Gly Ile Ala Leu Thr Leu Phe Asn Leu Ala Asp Thr Leu Leu Gly Gly 260 265 270 Leu Pro Thr Glu Leu Ile Ser Ser Ala Gly Gly Gln Leu Phe Tyr Ser 275 280 285 Arg Pro Val Val Ser Ala Asn Gly Glu Pro Thr Val Lys Leu Tyr Thr 290 295 300 Ser Val Glu Asn Ala Gln Gln Asp Lys Gly Ile Ala Ile Pro His Asp 305 310 315 320 Ile Asp Leu Gly Glu Ser Arg Val Val Ile Gln Asp Tyr Asp Asn Gln 325 330 335 His Glu Gln Asp Arg Pro Thr Pro Ser Pro Ala Pro Ser Arg Pro Phe 340 345 350 Ser Val Leu Arg Ala Asn Asp Val Leu Trp Leu Ser Leu Thr Ala Ala 355 360 365 Glu Tyr Asp Gln Ser Thr Tyr Gly Ser Ser Thr Gly Pro Val Tyr Val 370 375 380 Ser Asp Ser Val Thr Leu Val Asn Val Ala Thr Gly Ala Gln Ala Val 385 390 395 400 Ala Arg Ser Leu Asp Trp Thr Lys Val Thr Leu Asp Gly Arg Pro Leu 405 410 415 Ser Thr Ile Gln Gln Tyr Ser Lys Thr Phe Phe Val Leu Pro Leu Arg 420 425 430 Gly Lys Leu Ser Phe Trp Glu Ala Gly Thr Thr Lys Ala Gly Tyr Pro 435 440 445 Tyr Asn Tyr Asn Thr Thr Ala Ser Asp Gln Leu Leu Val Glu Asn Ala 450 455 460 Ala Gly His Arg Val Ala Ile Ser Thr Tyr Thr Thr Ser Leu Gly Ala 465 470 475 480 Gly Pro Val Ser Ile Ser Ala Val Ala Val Leu Ala Pro His Ser Ala 485 490 495 Leu Ala Gly Ser Leu Val Glu Glu Thr Ser Phe Ile Asp Ala Gly Ala 500 505 510 Pro 111617DNAArtificial SequenceHEV-HPV16 L2 chimeric gene (1617 bp) 11atgtctgcaa ctcagttgta taaaacttgc aagcaagctg gtacttgccc accagacatt 60atcccaaagg ttgaaggatc cgccgttgca cctgctcatg atactcctcc agttccagat 120gttgattcta gaggtgctat cttgagaaga caatacaacc ttagtacctc tcctttgact 180tcttccgttg ctactggtac aaatcttgtc ttgtacgcag ctccactttc acctcttttg 240ccattgcaag acggaaccaa cactcacatc atggctacag aagccagtaa ttatgctcag 300tacagagttg ccagagcaac tattagatat agacctttgg ttccaaacgc agtcggaggt 360tacgctattt ccatctcatt ctggccacaa accactacaa cccctacttc tgttgatatg 420aactctatca catcaaccga cgttagaatt ttggtccaac caggtatcgc ttctgagctt 480gttattcctt ccgaaagatt gcattataga aaccagggtt ggagatccgt tgaaacatca 540ggagtcgcag aagaggaagc tacctctggt cttgttatgt tgtgtattca cggaagtcca 600gtcaactctt atactaatac accttacact ggagcattgg gtcttttgga ttttgctctt 660gagttggagt ttagaaattt gactcctggt aacaccaaca ctagagtttc tagatactca 720agtactgcta gacatagatt gagaagagga gccgatggta ctgcagagtt gactacaacc 780gccgcaacaa gattcatgaa agacttgtac ttcacatcca ccaacggagt tggtgaaatt 840ggaagaggta tcgcccttac attgtttaat ttggcagata cccttttggg aggtcttcca 900actgagttga tttcttccgc tggaggtcaa ttgttctatt ctagaccagt tgtctccgct 960aacggagagc ctacagttaa attgtacacc tcagtcgaaa atgctcaaca ggataagggt 1020attgccatcc ctcatgatat cgacttggga gagtctagag ttgtcattca ggattacgac 1080aaccaacacg aacaggacag acctactcca tcccctgccc catctagacc attttctgtt 1140ttgagagcaa atgatgtcct ttggttgtca cttactgctg ccgaatatga ccaaagtact 1200tacggttcaa gtacaggacc tgtttatgtc agtgattctg ttaccttggt taacgtcgct 1260actggtgctc aggccgttgc aagatccttg gattggacta aggtcacact tgacggaaga 1320ccattgtcaa caattcaaca gtacagtaag acctttttcg ttttgcctct tcgtggtaaa 1380ttgtctttct gggaagccgg tactacaaag gcaggatacc catataacta caataccact 1440gcttccgatc aacttttggt tgagaatgca gctggtcaca gagtcgctat ctcaacttat 1500acaaccagtt tgggagccgg tccagtttcc atttcagctg ttgccgtcct tgctcctcat 1560tctgcattgg ctggatcctt ggttgaagaa acctccttta ttgacgctgg tgctcca 161712539PRTArtificial SequenceHEV-HPV16 L2 chimeric protein (539 AA) 12Met Ser Ala Thr Gln Leu Tyr Lys Thr Cys Lys Gln Ala Gly Thr Cys 1 5 10 15 Pro Pro Asp Ile Ile Pro Lys Val Glu Gly Ser Ala Val Ala Pro Ala 20 25 30 His Asp Thr Pro Pro Val Pro Asp Val Asp Ser Arg Gly Ala Ile Leu 35 40 45 Arg Arg Gln Tyr Asn Leu Ser Thr Ser Pro Leu Thr Ser Ser Val Ala 50 55 60 Thr Gly Thr Asn Leu Val Leu Tyr Ala Ala Pro Leu Ser Pro Leu Leu 65 70 75 80 Pro Leu Gln Asp Gly Thr Asn Thr His Ile Met Ala Thr Glu Ala Ser 85 90 95 Asn Tyr Ala Gln Tyr Arg Val Ala Arg Ala Thr Ile Arg Tyr Arg Pro 100 105 110 Leu Val Pro Asn Ala Val Gly Gly

Tyr Ala Ile Ser Ile Ser Phe Trp 115 120 125 Pro Gln Thr Thr Thr Thr Pro Thr Ser Val Asp Met Asn Ser Ile Thr 130 135 140 Ser Thr Asp Val Arg Ile Leu Val Gln Pro Gly Ile Ala Ser Glu Leu 145 150 155 160 Val Ile Pro Ser Glu Arg Leu His Tyr Arg Asn Gln Gly Trp Arg Ser 165 170 175 Val Glu Thr Ser Gly Val Ala Glu Glu Glu Ala Thr Ser Gly Leu Val 180 185 190 Met Leu Cys Ile His Gly Ser Pro Val Asn Ser Tyr Thr Asn Thr Pro 195 200 205 Tyr Thr Gly Ala Leu Gly Leu Leu Asp Phe Ala Leu Glu Leu Glu Phe 210 215 220 Arg Asn Leu Thr Pro Gly Asn Thr Asn Thr Arg Val Ser Arg Tyr Ser 225 230 235 240 Ser Thr Ala Arg His Arg Leu Arg Arg Gly Ala Asp Gly Thr Ala Glu 245 250 255 Leu Thr Thr Thr Ala Ala Thr Arg Phe Met Lys Asp Leu Tyr Phe Thr 260 265 270 Ser Thr Asn Gly Val Gly Glu Ile Gly Arg Gly Ile Ala Leu Thr Leu 275 280 285 Phe Asn Leu Ala Asp Thr Leu Leu Gly Gly Leu Pro Thr Glu Leu Ile 290 295 300 Ser Ser Ala Gly Gly Gln Leu Phe Tyr Ser Arg Pro Val Val Ser Ala 305 310 315 320 Asn Gly Glu Pro Thr Val Lys Leu Tyr Thr Ser Val Glu Asn Ala Gln 325 330 335 Gln Asp Lys Gly Ile Ala Ile Pro His Asp Ile Asp Leu Gly Glu Ser 340 345 350 Arg Val Val Ile Gln Asp Tyr Asp Asn Gln His Glu Gln Asp Arg Pro 355 360 365 Thr Pro Ser Pro Ala Pro Ser Arg Pro Phe Ser Val Leu Arg Ala Asn 370 375 380 Asp Val Leu Trp Leu Ser Leu Thr Ala Ala Glu Tyr Asp Gln Ser Thr 385 390 395 400 Tyr Gly Ser Ser Thr Gly Pro Val Tyr Val Ser Asp Ser Val Thr Leu 405 410 415 Val Asn Val Ala Thr Gly Ala Gln Ala Val Ala Arg Ser Leu Asp Trp 420 425 430 Thr Lys Val Thr Leu Asp Gly Arg Pro Leu Ser Thr Ile Gln Gln Tyr 435 440 445 Ser Lys Thr Phe Phe Val Leu Pro Leu Arg Gly Lys Leu Ser Phe Trp 450 455 460 Glu Ala Gly Thr Thr Lys Ala Gly Tyr Pro Tyr Asn Tyr Asn Thr Thr 465 470 475 480 Ala Ser Asp Gln Leu Leu Val Glu Asn Ala Ala Gly His Arg Val Ala 485 490 495 Ile Ser Thr Tyr Thr Thr Ser Leu Gly Ala Gly Pro Val Ser Ile Ser 500 505 510 Ala Val Ala Val Leu Ala Pro His Ser Ala Leu Ala Gly Ser Leu Val 515 520 525 Glu Glu Thr Ser Phe Ile Asp Ala Gly Ala Pro 530 535 1340DNAArtificial SequenceHEVFP PCR PRIMER 13catttgaatt caccatggcc gttgcacctg ctcatgatac 401439DNAArtificial SequenceHEVRP PCR PRIMER 14tatcgcggcc gctcattaag ccaatgcaga atgaggagc 391540DNAArtificial SequenceL2NTFP 15atgtcgaatt caccatggct gcaactcagt tgtataaaac 401632DNAArtificial SequenceL2NTRP 16atcgaggatc cttgaacctt tgggataatg tc 321734DNAArtificial SequenceL2CTFP PCR PRIMER 17atgtcggatc ctctgcaact cagttgtata aaac 341843DNAArtificial SequenceL2CTRP PCR PRIMER 18atcgagcggc cgctcattaa ccttcaacct ttgggataat gtc 431939DNAArtificial SequenceL2CTRP1 PCR PRIMER 19ttggttgaag aaacctcctt tattgacgct ggtgctcca 392035DNAArtificial SequenceHEVNTFP PCR PRIMER 20acgtcggatc catcgccctt acattgttta atttg 352139DNAArtificial SequenceHEVNTRPPCR PRIMER 21tatcgcggcc gctcattaag ccaatgcaga atgaggagc 392238DNAArtificial SequenceHEVCTFP PCR PRIMER 22agctcgaatt caccatggcc cttacattgt ttaatttg 382338DNAArtificial SequenceHEVCTRP PCR PRIMER 23actcaggatc cttatcaagc caatgcagaa tgaggagc 38

Claims

1. Vaccine composition useful for administration to humans comprising: (i) a diphtheria toxoid, `D`; (ii) a tetanus toxoid, `T`; (iii) pertussis antigens; (iv) recombinant hepatitis B virus surface antigen, HBsAg; (v) recombinant human papillomavirus L1 antigens of HPV16 and HPV18; (vi) recombinant hepatitis E (HEV) ORF2 antigen; (vii) recombinant HPV L2 epitope in chimeric fusion with HBsAg or Hepatitis E (HEV) protein.

2. The vaccine composition as claimed in claim 1, wherein components include the hepatitis E ORF2 comprising the 112-606 amino acids of the protein of SEQ ID NO: 4 encoded by the gene of SEQ ID NO: 3.

3. The vaccine composition as claimed in claim 1, wherein the heterologous HPV L2 epitope is fused at any position along the HEV ORF2 protein preferably at the N-terminus end such as in SEQ ID NO: 6 encoded by SEQ ID NO: 5.

4. The vaccine composition as claimed in claim 1, wherein the heterologous HPV L2 epitope is fused at any position along the HEV protein, preferably at the C-terminus end such as in SEQ ID NO: 8 encoded by SEQ ID NO: 7.

5. The vaccine composition as claimed in claim 1, wherein the recombinant antigens HEV and chimeric HEV-L2 antigens are encoded by nucleotide sequences SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9 and SEQ ID NO: 11 that are codon optimized for enhanced expression in Pichia pastoris and encode respectively the proteins of SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10 and SEQ ID NO: 12.

6. The vaccine composition as claimed in claim 5, wherein the recombinant antigens are cloned, expressed and purified from yeast cells preferably Pichia pastoris.

7. The vaccine composition as claimed in claim 1, further comprising an adjuvant.

8. The vaccine composition as claimed in claim 7, wherein the adjuvant is alum, selected from aluminum hydroxide or aluminum phosphate, and gamma inulin and algammulin.

9. A vaccine composition useful for administration to humans comprising: (a) a first component comprising HEV, HPV and chimeric HEV or HBsAg antigens; and (b) a second component comprising Tdap.

10. A method of combining the vaccine antigens as claimed in claim 9 for concomitant administration comprising the steps of: (a) providing a first component comprising HEV, HPV and chimeric HEV or HBsAg antigens; (b) providing a second component comprising Tdap antigens; and (c) mixing the first and second components to give the vaccine.

11. A vaccine composition according to claim 9, wherein Tdap can be formulated in aluminum hydroxide and used as a single component vaccine.

12. A method of producing the recombinant antigens of claim 5, in yeast cells wherein the genes encoding the recombinant proteins are cloned in a yeast expression vector and expressed as intracellular proteins in yeast cells and purified therefrom.

13. A method for eliciting and measuring immune response against one or more antigens of claim 1 by administering vaccine doses parenterally, and measuring the antibody titer by ELISA.

14. A method of producing the recombinant antigens of claim 6, in yeast cells wherein the genes encoding the recombinant proteins are cloned in a yeast expression vector and expressed as intracellular proteins in yeast cells and purified therefrom.

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